A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134933



Internal ID20701973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90580456..90580873hg38UCSC Ensembl
chr5:89876273..89876690hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414429
Supporting Variants
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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